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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297607Generated: October 28, 2026

N-bromobutanimide → 7-Amino-8-bromo-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/2297607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 18382547HCID 18382547—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-Amino-8-bromo-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinolineHCID 18382561—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 7-amino-2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinoline from D3 (7 g) in acetonitrile (200 ml), was added N-bromo succinimide (7.21 g) portionwise over 10 min. The reaction mixture was cooled in an ice/methanol bath to prevent any large exotherm. and then stirred under argon for 45 min. The reaction was allowed to warm to 25° C., diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and evaporated to dryness in vacuo. The resultant brown solid was purified using dry flash column chromatography with ethyl acetate. Combination of appropriate fractions gave the title compound as an orange gum (3.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492378B1
Source datasetuspto-grants-2002_12
ORD IDord-f2961e842fcf43a081945c59f309fab6
Source noteuspto-grants-2002_12